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HRID 2035866作成日:2026年10月26日

9-[4-(3-Methylphenoxy)phenyl]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide → 9-[4-(3-Methylphenoxy)phenyl]-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/2035866

反応式

関与物質

役割名称HCID仕込み量
反応物9-[4-(3-Methylphenoxy)phenyl]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 66748857—
触媒Adams' catalystHCID 345198—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物9-[4-(3-Methylphenoxy)phenyl]-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 6674847967.5%

反応条件

温度50 °C

反応手順

Platinum(IV) oxide (30 mg) was added to a solution of 9-[4-(3-methylphenoxy)phenyl]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide (357 mg) in THF (dry) (80 mL) and MeOH (80 ml) and the mixture was stirred at 50° C. under hydrogen for 6 hr. Activated carbon was added and the insoluble solid was removed by filtration through NH-silica gel/Celite pad (eluted with EtOAc) and the filtrate was concentrated in vacuo. The residue was crystallized from MeCN-THF/IPE to give the title compound (243.5 mg) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08575154B2
出典データセットuspto-grants-2013_11
ORD IDord-e06df37dc7e34940a02173e7669368eb
出典メモuspto-grants-2013_11